CSV Auditor

Advarra, Inc.; Remote; GBP 52,000 - 71,000; Part time

Job summary

A leading clinical research organization is seeking CSV Auditors to join their consultant network. Candidates will conduct audits, ensure compliance with regulations, and collaborate with client teams. The ideal candidate has at least 10 years of Quality Assurance experience and 5 years in auditing. This role is open to candidates in the EU region.

Qualifications

• Minimum 10 years of experience in Quality Assurance and/or GxP in life sciences.
• Minimum 5 years of experience in Quality Assurance auditing.

Responsibilities

• Conduct Computer System Validation (CSV) audits for life science clients.
• Assess compliance with GxP regulations and client requirements.
• Develop audit reports and provide recommendations.
• Collaborate with client teams to ensure remediation actions are implemented.

Skills

Quality Assurance

GxP regulations knowledge

Interpersonal skills

Verbal communication in English

Written communication in English

Job description

At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each person is not only valued but empowered to thrive and make a meaningful impact.

Company Culture

Our people--both employees and consultants—are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.

Job Overview Summary

Advarra is seeking CSV Auditors to join our consultant network for EU-based projects. Auditors ensure compliance with GxP regulations and provide expertise across clinical, laboratory, and manufacturing systems.

Job Duties & Responsibilities

• Conduct Computer System Validation (CSV) audits for life science clients.
• Assess compliance with GxP regulations and client requirements.
• Develop audit reports and provide recommendations.
• Collaborate with client teams to ensure remediation actions are implemented.

Location

This evergreen role is open to candidates based in the EU region.

Basic Qualifications

• Minimum ten (10) years of Quality Assurance and/or GxP experience in life sciences.
• Minimum five (5) years of Quality Assurance auditing experience.
• Strong interpersonal and client interaction skills.
• Excellent verbal and written communication in English.